FdaApplication
ANDA 209356
Identifiers
- fda_app_no: ANDA209356
Properties
| Property | Value |
|---|---|
| applicant_name | AMNEAL PHARMACEUTICALS LLC |
| application_type | ANDA |
| approval_date | 2019-12-02 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| SUCRALFATE | SUCRALFATE | 1GM/10ML | SUSPENSION;ORAL |
1 product